Canonical Allele Identifier: PA2580203419
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1793244
ClinVar RCV Id: RCV002452765
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu857Pro
CA382543857
NM_001351834.2:c.2570T>C